U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 122

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5283669copy number variation1nstd204human GRCh38.p13 chr17: 39,851,001-40,379,500 , GRCh37.p13 chr17: 38,007,254-38,535,752 , CASC3, 27 more genes
    nsv5194528mobile element insertion1nstd203human GRCh38 chr17: 40,339,708-40,339,708 , GRCh37.p13 chr17: 38,495,960-38,495,960 RARA, RARA-AS1
    nsv5190245mobile element insertion1nstd203human GRCh38 chr17: 40,339,693-40,339,705 , GRCh37.p13 chr17: 38,495,945-38,495,957 RARA-AS1, RARA
    nsv4628986copy number variation1nstd183human GRCh37 chr17: 38,215,916-38,530,107 , GRCh38.p12 chr17: 40,059,663-40,373,855 PPIAP54, MSL1, 14 more genes
    nsv4619124copy number variation1nstd183human GRCh37 chr17: 38,474,645-38,499,036 , GRCh38.p12 chr17: 40,318,393-40,342,784 LOC105371934, RARA, 1 more genes
    nsv4576383mobile element insertion1nstd166human GRCh37.p13 chr17: 38,495,945-38,495,945 , GRCh38.p12 chr17: 40,339,693-40,339,693 RARA-AS1, RARA
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 more genes
    nsv4334447sequence alteration1nstd166human GRCh37.p13 chr17: 38,428,364-38,577,561 , GRCh38.p12 chr17: 40,272,112-40,421,309 WIPF2, PPIAP54, 8 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4267755copy number variation1nstd166human GRCh37.p13 chr17: 38,483,228-38,503,086 , GRCh38.p12 chr17: 40,326,976-40,346,834 RARA-AS1, RARA
    nsv3958649copy number variation1nstd168human GRCh38 chr17: 40,325,908-40,346,749 , GRCh37.p13 chr17: 38,482,160-38,503,001 RARA, RARA-AS1
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 PRPSAP1, CACNG1, 1350 more genes
    nsv3911563copy number variation1nstd102humanPathogenic NCBI36 chr17: 45,918,236-63,677,950 , GRCh37 chr17: 48,563,237-65,936,105 , GRCh38 chr17: 36,449,220-68,170,214 PLEKHH3, CHCT1, 958 more genes
    nsv3911344copy number variation1nstd102humanPathogenic GRCh37 chr17: 37,356,126-43,706,945 , NCBI36 chr17: 34,609,652-41,062,728 , GRCh38 chr17: 39,199,873-45,629,579 IFI35, RND2, 345 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 MIR21, LOC105371899, 2366 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 MIR3185, YWHAEP6, 2366 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center